- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED data as of Jul 30, 2026
EUDAMED last updated this device on Jul 22, 2026
590571804podortQCPoduszka ortopedyczna Kneeva is an EU MDR-regulated medical device on the European market. It is classified as Class I. Manufactured by GOODWILL BRANDS sp. z o.o.. Placed on the EU market in Poland. Explore certificates, regulatory status and the official record on MD Atlas.
05905718041169Kneeva, biała(01)05905718041169
European Medical Device Nomenclature — the EU product classification assigned to this device.
V080302PATIENT POSITIONING MEDICAL CUSHIONSPL-MF-000054023The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | — | Still on market |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
No certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.590571804podortQCOn the marketPoduszka ortopedyczna B-Dream590571804podortQCOn the marketPoduszka ortopedyczna B-Dream590571804podortQCOn the marketPoduszka ortopedyczna ZenFlex590571804podortQCOn the marketPoduszka ortopedyczna ZenFlex590571804podortQCOn the marketPoduszka ortopedyczna ZenFlex590571804podortQCOn the market